Service Line TransPerc

Overview

Información sobre este estudio

The purpose of this study is to compare transcutaneous electrical spinal stimulation and epidural electrical spinal stimulation.  Relationships between stimulation input and electrophysiological output will be recorded, and changes in motor, sensory, and functional outcomes during and after stimulation will be assessed.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

- Spinal cord injury due to trauma located at or above the tenth thoracic vertebrae
(T10)

- American Spinal Injury Association grading scale of A-D (2 from each) below the level
of SCI

- Intact spinal reflexes below the level of SCI

- At least 1-year post-SCI

- At least 22 years of age

- Willing to use medically acceptable methods of contraception, if female and of
child-bearing potential

Exclusion Criteria:

- Currently a prison inmate, or awaiting trial, related to criminal activity

- Pregnancy at the time of enrollment

- History of chronic and/or treatment resistant urinary tract infection

- Unhealed decubitus ulcer

- Unhealed skeletal fracture

- Untreated clinical diagnosis of depression

- Undergoing, or planning to undergo, diathermy treatment

- Active participation in another interventional clinical trial

- Presence of conditions or disorders which require MRI monitoring

- A history of coagulopathy or other significant cardiac or medical risk factors for
surgery

- Current use of a ventilator

- Clinically diagnosed cardiopulmonary complications such as chronic obstructive
pulmonary disease, cardiac failure, or heart arrhythmia that contraindicate changes in
body position such as supine-to-sit-to-stand activities, prolonged standing, or
stepping

- History of frequent hypotension characterized by light headedness, or loss of
consciousness

- History of frequent hypertension characterized by headache, or bradycardia

- History of frequent, severe, autonomic dysreflexia

- Any illness or condition which, based on the research team's assessment, will
compromise with the patient's ability to comply with the protocol, patient safety, or
the validity of the data collected during this study.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 12/20/22. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Kristin Zhao, Ph.D., M.S.

Cerrado para la inscripción

Contact information:

Tyson Scrabeck CCRP

(507) 538-1016

Scrabeck.Tyson@mayo.edu

More information

Publicaciones

Publications are currently not available
.
CLS-20520842

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